WO2021073910A1 - Cire de son de riz brillant oxydée avec une teneur élevée en esterane - Google Patents

Cire de son de riz brillant oxydée avec une teneur élevée en esterane Download PDF

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Publication number
WO2021073910A1
WO2021073910A1 PCT/EP2020/077785 EP2020077785W WO2021073910A1 WO 2021073910 A1 WO2021073910 A1 WO 2021073910A1 EP 2020077785 W EP2020077785 W EP 2020077785W WO 2021073910 A1 WO2021073910 A1 WO 2021073910A1
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Prior art keywords
rice bran
bran wax
oxidate
wax oxidate
total weight
Prior art date
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PCT/EP2020/077785
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German (de)
English (en)
Inventor
Philipp KRATZER
Manuel BROEHMER
Rainer Fell
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Clariant International Ltd
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Application filed by Clariant International Ltd filed Critical Clariant International Ltd
Priority to EP20781549.9A priority Critical patent/EP4045599A1/fr
Priority to BR112022003064A priority patent/BR112022003064A2/pt
Priority to CN202080072171.9A priority patent/CN114555715B/zh
Priority to JP2022521965A priority patent/JP7470188B2/ja
Priority to US17/768,238 priority patent/US20240117187A1/en
Priority to KR1020227016328A priority patent/KR20220084345A/ko
Publication of WO2021073910A1 publication Critical patent/WO2021073910A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06—Waxes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/02—Printing inks
    • C09D11/12—Printing inks based on waxes or bitumen
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D191/00—Coating compositions based on oils, fats or waxes; Coating compositions based on derivatives thereof
    • C09D191/06—Waxes

Definitions

  • the invention relates to light-colored rice bran wax oxidates with a high ester content and a medium acid number, a process for the production of these oxidation products of rice bran wax and their use for agricultural or forestry purposes, as an additive in plastics processing, in care products, in printing inks and / or in paints.
  • the subject is also saponified rice bran wax oxidates, produced by saponifying the rice bran wax oxidates according to the invention.
  • Oxidation with chromosulfuric acid leads to lighter wax products.
  • the chromic acid bleaching of these natural waxes usually leads to high acid numbers, typically in the range from 130 to 160 mg KOH / g.
  • Oxidation with chromic acid essentially results in cleavage of the wax esters and in situ oxidation of the wax alcohols formed to form wax acids.
  • the acid number is a measure of the content of free wax acids. The typical conversions of such oxidations are in the range of 50-90% with respect to the ester groups.
  • the natural waxes bleached in this way have, in addition to the desired lightening, a higher saponification number and acid number than the unbleached waxes, which is undesirable for some applications.
  • rice bran wax oxidates with a higher acid number can be more easily derivatized, for example by esterification. For some applications it is advantageous if the acid number remains relatively low, but is still high enough to enable derivatizations to a significant extent.
  • the acid number of the wax oxidates can be reduced, for example, by esterifying the acids contained in the wax and / or wax oxidate with alcohols.
  • This esterification is often carried out with polyvalent alcohols such as ethylene glycol, butylene glycol or glycerine. However, this involves an additional step that is disadvantageous for reasons of process economy.
  • rice bran wax is a by-product of the processing of paddy rice (oryza sativa) in large quantities. After the lemmas adhering to the grains have been removed during the threshing of the ripe rice plants and further husk components and other impurities have been separated in the rice mill, the rice grains still contain the seedling and are enclosed by the silver skin. The seedling and silver skin are removed in a further processing step by grinding and deliver the rice bran in addition to the milled rice.
  • the rice bran contains lipid components, which mainly consist of fatty oils and a smaller percentage of waxy components.
  • the waxy components are found in the oil obtained from the bran by pressing or solvent extraction, from which they can be isolated due to their poor solubility at low temperatures, e.g. by freezing.
  • the calculated potential availability of rice bran wax is around 300,000 tons per year.
  • rice bran wax belongs to a group of waxes that so far have only been of local importance or only of academic interest.
  • the use of rice bran wax in cosmetics has been described (EP-A 1343454; B syndrometigam, Lexikon der kosmetischen Rohstoffe, Norderstedt 2010, p. 77), as a processing aid in plastics (JP-A H10-007862 (1998); JP-A S60- 011553 (1985); JP-A S49-090739 (1974)) and in printing inks and electrophotographic toners (JP-A 2010-020304; 2010).
  • the rice bran wax esters mainly consist of monoesters of long-chain, saturated, unbranched monocarboxylic acids with long-chain, unbranched, aliphatic monoalcohols (hereinafter also referred to as "genuine esters").
  • the acid content of the rice bran wax esters behenic and lignoceric acid, with chain lengths C22 and C24, and in the alcohol content of the rice bran wax esters, the chain lengths C26, C28, C30, C32 and C34 are predominant.
  • the wax can also contain free fatty acids and other components such as squalene, phospholipids and steryl esters.
  • the content of wax esters in refined and de-oiled rice bran wax is generally greater than 96% by weight.
  • the content of wax esters depending on the content of the rice bran oil, can also be as low as 50% by weight.
  • Other variable components of the rice bran wax that are to be regarded as “small quantities” are the unspecified “dark substances”, squalene and the so-called “gum component”. These components usually lead to a product quality that fluctuates in terms of color and applicability and is difficult to reproduce.
  • CN-A 108048222, CN-A 108129302 and CN-A 108191602 from 2018 describe rice bran wax oxidates that are produced from de-oiled rice bran wax by oxidation with sodium dichromate, esterified with a polyhydric alcohol (CN-A 108129302 and CN-A 108191602) and then saponified (CN-A 108191602).
  • CN-A 108129302 and CN-A 108191602 esterified with a polyhydric alcohol
  • saponified CN-A 108191602
  • EP-A 2909273 from 2015 discloses oxidation products of rice bran wax, produced by oxidation with chromic acid in the presence of oxidation promoters such as fluorinated alkylsulfonic acids, aluminum trichloride or hydrochloric acid, or with particularly vigorous stirring. As a result, high acid numbers are aimed for.
  • EP-A 2909274 describes rice bran wax oxidates which are saponified before the oxidation. Here, too, high acid numbers are achieved.
  • JP-B S36-005526 (1961) describes the production of solvent-based polishing compounds which contain a chemically modified wax based on rice bran wax. The modification takes place through the oxidation of raw rice bran wax with chromic acid or dichromate salts. Acid numbers of 40-45 mg KOH / g are achieved.
  • ester waxes have the desired acid number without the need for an additional esterification step.
  • Such compounds could previously only be obtained by oxidation of rice bran wax to acid numbers in the range of about 140 mg KOFI / g and subsequent esterification with multiple alcohols (EP-A 2909274).
  • the invention therefore relates to a process for the production of rice bran wax oxidates (O) with an acid number of greater than 45 mg KOFI / g and less than 70 mg KOFI / g, comprising the steps: i) providing a rice bran wax (R) containing less than 5% by weight, based on the total weight of the rice bran wax (R), of multiple esters formed from polyhydric alcohols and aliphatic carboxylic acids with 8 to 20 carbon atoms; ii) providing a mixture (M) of chromium trioxide and sulfuric acid; iii) performing the oxidation of the rice bran wax (R) by reacting the rice bran wax (R) with the mixture (M) with stirring and at a temperature of 90 to 150 ° C to obtain a rice bran wax oxidate (O); iv) ending the reaction and allowing the reaction mixture obtained in step iii) to rest until the organic phase is separated from the aqueous phase; v) separation of the
  • the rice bran wax (R) provided in step i) can be any rice bran wax, provided it has a proportion of multiple esters, formed from polyhydric alcohols and aliphatic carboxylic acids with 8 to 20 carbon atoms, of less than 5% by weight, preferably less than 2% by weight, particularly preferably 0.1 to 2% by weight, based on the total weight of the rice bran wax (R).
  • the desired proportion of multiple esters formed from polyhydric alcohols and aliphatic carboxylic acids with 8 to 20 carbon atoms can already be contained in the raw rice bran wax, but can also be adjusted by pretreating the rice bran wax.
  • the proportion is preferably already contained in the raw rice bran wax (R). In this case, it is preferred that the rice bran wax (R) is not pretreated.
  • the rice bran wax (R) must be pretreated before being provided in step i). In this case it is advantageous if the pretreatment does not include saponification of the esters contained in the rice bran wax (R).
  • an extraction of the multiple esters formed from polyhydric alcohols and aliphatic carboxylic acids with 8 to 20 carbon atoms with one or more organic solvents is preferred, the extraction being carried out until the desired proportion of multiple esters, formed from polyhydric alcohols and aliphatic carboxylic acids with 8 up to 20 carbon atoms, of less than 5% by weight is achieved.
  • Any organic solvents which can dissolve oils and fats are suitable, for example ethyl acetate or acetone, preferably ethyl acetate.
  • the multiple esters formed from polyhydric alcohols and aliphatic carboxylic acids with 8 to 20 carbon atoms, are preferably di- and tri-glycerides of aliphatic carboxylic acids with 8 to 20 carbon atoms, especially oils that are naturally contained in rice bran, especially rice bran oil.
  • the extraction with an organic solvent can involve de-oiling.
  • the proportion of multiple esters, formed from polyhydric alcohols and aliphatic carboxylic acids with 8 to 20 carbon atoms, of less than 5% by weight can also be referred to as the oil content of the rice bran wax.
  • the rice bran wax (R) regardless of the proportion of multiple esters formed from polyhydric alcohols and aliphatic carboxylic acids having 8 to 20 carbon atoms in the raw state, is preferably not pretreated by saponification at any time before the oxidation.
  • the mixture (M) of chromium trioxide and sulfuric acid provided in step ii) can be any mixture, provided it is able to oxidize oxidizable constituents of rice bran wax. Such mixtures of chromium trioxide and sulfuric acid are often referred to as chromosulfuric acid.
  • the sulfuric acid is concentrated sulfuric acid with a sulfuric acid content of at least 90% by weight, preferably at least 96% by weight, particularly preferably at least 99% by weight. This can optionally be fuming sulfuric acid, i.e. it can also contain sulfur trioxide.
  • the concentration of chromium trioxide in the mixture (M) is preferably 50 to 200 g / L, particularly preferably 70 to 150 g / L, very particularly preferably 80 to 120 g / L.
  • step iii) of the process according to the invention the oxidation of the rice bran wax (R) by reacting the rice bran wax (R) with the mixture (M) with stirring and at a temperature of 80 to 150 ° C, preferably 90 to 140 ° C, is particularly preferably carried out at from 105 to 130 ° C to obtain a rice bran wax oxidate (O).
  • the weight ratio of total chromium trioxide used to rice bran wax (R) used is preferably from 5: 4 to 2: 1 (1.25 to 2), in particular from 13:10 to 17:10 (1.3 to 1.7). If the ratio is less than 5: 4, it will be too low Acid numbers reached. If the ratio is greater than 2: 1, acid numbers that are too high are reached.
  • step iii) can comprise the initial charge of the mixture (M) and then adding the rice bran wax (R).
  • step iii) can comprise the initial charge of the rice bran wax (R) and then adding the mixture (M).
  • the respective second component (R) or (M) can be added in portions, continuously or in one batch, preferably in portions or continuously, particularly preferably in portions.
  • the temperature of the rice bran wax (R) and / or the mixture (M) during the addition can deviate from the reaction temperature and only after the addition of the second component to the required value of 80 to 150 ° C, preferably 90 to 140 ° C , particularly preferably from 105 to 130 ° C.
  • the temperature during the addition can be from 70 to 130.degree. C., preferably from 80 to 110.degree.
  • the rice bran wax (R) is in molten form during the addition.
  • the prepared mixture (M) of chromium trioxide and sulfuric acid is initially introduced and heated to a temperature of 70 to 130 ° C., and the solid rice bran wax (R) is added in portions. After the addition has taken place, the temperature is adjusted to 80 to 150 ° C. and the oxidation is carried out.
  • the prepared mixture (M) of chromium trioxide and sulfuric acid is initially introduced and heated to a temperature of 70 to 130 ° C., and the rice bran wax (R) in the molten state, preferably at a temperature of 70 to 130 ° C., in portions admitted. After the addition has taken place, the temperature is adjusted to 80 to 150 ° C. and the oxidation is carried out.
  • the rice bran wax (R) is initially introduced and melted at a temperature of 70 to 130 ° C., and the mixture (M) of chromium trioxide and sulfuric acid is added cold in portions.
  • the temperature is adjusted to 80 to 150 ° C. and the oxidation is carried out.
  • the rice bran wax (R) is initially introduced and melted at a temperature of 70 to 130 ° C, and the mixture (M) of chromium trioxide and sulfuric acid is added hot in portions, preferably at a temperature of 70 to 130 ° C. After the addition has taken place, the temperature is adjusted to 80 to 150 ° C. and the oxidation is carried out.
  • rice bran wax (R) and the mixture (M) of chromium trioxide and sulfuric acid are initially introduced together at room temperature and slowly heated to a temperature of 80 to 150 ° C., and the oxidation is carried out at this temperature.
  • At least the oxidation at 80 to 150 ° C. preferably also the addition of the rice bran wax (R) and / or the mixture (M), takes place with stirring.
  • the stirring can take place in any way, for example with a mechanically operated agitator or a magnetically operated agitator.
  • the stirring is preferably carried out with a mechanically operated agitator, particularly preferably with a mechanically operated agitator comprising a KPG stirrer.
  • the stirring speed in step iii) is preferably in a range from 100 to 500 rpm (revolutions per minute), particularly preferably from 120 to 300 rpm, very particularly preferably from 170 to 250 rpm, since a stirring speed below 100 rpm the mixing required for efficient oxidation is not given and at a stirring speed of over 500 rpm there is an increased risk of the formation of an inseparable emulsion.
  • the oxidation of the rice bran wax in step iii) at the temperature of 90 to 150 ° C. takes place over a period of 1 to 8 hours, preferably from 2 to 5 hours, particularly preferably from 3 to 4.5 hours.
  • no oxidation promoters are added to the reaction mixture of rice bran wax (R) and the mixture (M), since these can often lead to the cleavage of the ester bonds and therefore can increase the acid number in the rice bran wax oxidate (O). It is therefore preferable not to use any oxidation promoters, in particular no oxidation promoters such as emulsifiers (e.g. alkanesulfonates, fluorinated alkanesulfonates), surfactants, polymeric surfactants, nitrogen-containing cationic surfactants, phase transfer catalysts, Fenton reagents, metal salts, hydrochloric acid or the like in the oxidation.
  • emulsifiers e.g. alkanesulfonates, fluorinated alkanesulfonates
  • surfactants e.g. alkanesulfonates, fluorinated alkanesulfonates
  • polymeric surfactants e.g. alkanesul
  • step iv) the reaction mixture is left to stand until the organic phase has separated from the aqueous phase.
  • “Ending the reaction” means that the stirring is interrupted and the heating is ended. This begins the separation of the floating organic phase, containing the rice bran wax oxidate (O), from the sinking aqueous phase, containing sulfuric acid and chromium compounds.
  • the reaction mixture can optionally be transferred to a device in which, after the separation of the organic phase from the aqueous phase, separation of the organic phase is facilitated.
  • a separatory funnel An example of such a device is a separatory funnel. Other devices for this purpose are known to the person skilled in the art and can be used here.
  • step v) the organic phase containing the rice bran wax oxidate is separated off. This can be done, for example, using a separating funnel. Alternatively, the floating organic phase can be skimmed off using suitable technical means. It is also possible to pour off the organic phase over a vessel rim. Ways of separating organic phases from aqueous phases after phase separation are known in principle to the person skilled in the art and can be used here. Furthermore, in step vi), the separated organic phase containing the rice bran wax oxidate can optionally be worked up further in order to remove residues containing chromium compounds from the organic phase and thus obtain the rice bran wax oxidate in purified form.
  • the work-up can be carried out in any way that is suitable for the separation of polar and / or water-soluble substances from organic substances.
  • the organic phase can be purified by chromatography or filtered through silica gel.
  • Residues containing chromium compounds are preferably removed by washing the organic phase with an aqueous solution of oxalic acid and / or sulfuric acid.
  • residues containing chromium compounds can preferably be removed by washing the organic phase with water.
  • residues containing chromium compounds can preferably be removed by centrifuging the organic phase. “Washing” here is to be understood in each case as the mixing of the organic phase with the respective washing agent and subsequent phase separation in accordance with steps iv) and v).
  • residues containing chromium compounds are removed by washing the organic phase one or more times with an aqueous solution of oxalic acid and sulfuric acid, followed by washing the organic phase one or more times with water.
  • residues containing chromium compounds are removed by one or more times Washing the organic phase with an aqueous solution of oxalic acid and sulfuric acid, followed by centrifuging the organic phase.
  • residues containing chromium compounds are removed by washing the organic phase one or more times with water, followed by centrifuging the organic phase.
  • residues containing chromium compounds are removed by washing the organic phase one or more times with an aqueous solution of oxalic acid and sulfuric acid, followed by washing the organic phase one or more times with water, followed by centrifuging the organic phase.
  • step vii) the sequence of steps ii) to vi) can be repeated up to two times, the rice bran wax oxidate (O), optionally in purified form, being used instead of the rice bran wax (R).
  • the sequence of steps ii) to vi) is preferably repeated up to one time in step vii). In these cases, when steps ii) to vi) are carried out for the first time, at least half of the total chromium trioxide provided is used, and when steps ii) to vi) are repeated, the remaining part.
  • the sequence of steps ii) to vi) is particularly preferably not repeated.
  • the invention also relates to a rice bran wax oxidate (O) with an acid number (measured according to DIN ISO 2114 of 2002) greater than 45 mg KOH / g and less than 70 mg KOH / g, produced by the process according to the invention.
  • the rice bran wax oxidate preferably has an acid number greater than 45 mg KOH / g and less than 65 mg KOH / g.
  • the invention also relates to a rice bran wax oxidate (O) with an acid number greater than 45 mg KOH / g and less than 70 mg KOH / g, preferably less than 65 mg KOH / g and with a proportion of multiple esters polyhydric alcohols and aliphatic carboxylic acids with 22 to 36 carbon atoms less than 5% by weight, based on the total weight of the rice bran wax oxidate (O).
  • O rice bran wax oxidate
  • the rice bran wax oxidate (O) preferably has a proportion of multiple esters formed from polyhydric alcohols and aliphatic carboxylic acids with 22 to 36 carbon atoms less than 5% by weight, particularly preferably less than 3% by weight, very particularly preferably less than 1% by weight .-%, based on the total weight of the rice bran wax oxidate (O).
  • the rice bran wax oxidate (O) contains a) 10 to 40% by weight, based on the total weight of the rice bran wax oxidate (O), of free aliphatic carboxylic acids having 8 to 36 carbon atoms; b) 0 to 5% by weight, based on the total weight of the rice bran wax oxidate (O), of free aliphatic alcohols having 24 to 36 carbon atoms; c) 0 to 10% by weight, based on the total weight of the rice bran wax oxidate (O), of free aliphatic dicarboxylic acids having 10 to 30 carbon atoms; d) 45 to 90% by weight, based on the total weight of the rice bran wax oxidate (O), genuine esters with 42 to 64 carbon atoms; and e) 0 to 15% by weight, based on the total weight of the rice bran wax oxidate (O), of further natural constituents contained in the rice bran wax.
  • the rice bran wax oxidate (O) contains a) 13 to 35% by weight, based on the total weight of the rice bran wax oxidate (O), of free aliphatic carboxylic acids having 8 to 36 carbon atoms; b) 0 to 3% by weight, based on the total weight of the rice bran wax oxidate (O), of free aliphatic alcohols having 24 to 36 carbon atoms; c) 0 to 4% by weight, based on the total weight of the rice bran wax oxidate (O), of free aliphatic dicarboxylic acids having 10 to 30 carbon atoms; d) 50 to 87% by weight, based on the total weight of the rice bran wax oxidate (O), genuine esters with 42 to 64 carbon atoms; and e) 0 to 15% by weight, based on the total weight of the rice bran wax oxidate (O), of further natural components contained in the rice bran wax.
  • the rice bran wax oxidate (O) contains a) 15 to 30% by weight, based on the total weight of the rice bran wax oxidate (O), of free aliphatic carboxylic acids having 8 to 36 carbon atoms; b) 0 to 1% by weight, based on the total weight of the rice bran wax oxidate (O), of free aliphatic alcohols having 24 to 36 carbon atoms; c) 0 to 3% by weight, based on the total weight of the rice bran wax oxidate (O), of free aliphatic dicarboxylic acids having 10 to 30 carbon atoms; d) 55 to 85% by weight, based on the total weight of the rice bran wax oxidate (O), genuine esters with 42 to 64 carbon atoms; and e) 0 to 15% by weight, based on the total weight of the rice bran wax oxidate (O), of further natural constituents contained in the rice bran wax.
  • lignoceric acid is preferably contained in the rice bran wax oxidate (O) to a maximum of 5% by weight, particularly preferably a maximum of 3% by weight, based on the total weight of the rice bran wax oxidate (O).
  • the weight fractions and chain length distributions can be measured, for example, by means of gas chromatography.
  • the rice bran wax oxidates according to the invention typically have a dropping point measured according to DIN ISO 2176 (1997) between 70 ° C and 90 ° C, preferably between 75 ° C and 80 ° C.
  • the rice bran wax oxidates according to the invention preferably have a particularly light to white color compared to conventional oxidates (eg montan wax base).
  • the color can be determined using the iodine color number measured according to DIN 6162 (2014).
  • it is less than 20, preferably less than 6, in particular less than 2.
  • the rice bran wax oxidates according to the invention preferably have a needle penetration number (NPZ) measured according to DIN 51579 (2010) of less than 10 mm -1 , preferably less than 5 mm -1 , particularly preferably less than 3 mm -1 .
  • the oxidation of the rice bran wax preferably increases the saponification number, measured in accordance with DIN ISO 3681 (2007), by at most 40%, preferably by at most 30%, particularly preferably by at most 20%.
  • the increase in the saponification number can be explained mechanistically by the cleavage of the wax esters and the subsequent oxidation of the wax alcohols to acids.
  • some of the unsaturated carbon-carbon bonds are split by the oxidizing agent and also oxidized to acids.
  • the saponification number is thus also a measure of the oxidation that actually took place, as opposed to saponification, in which the saponification number does not change, as is known, and as opposed to other bleaching processes in which the product is only lightened.
  • the bleaching of rice bran wax with hydrogen peroxide does not cause any chemical modification of the wax in the sense of the invention, since here only discolouring impurities and secondary constituents are removed without changing the actual wax structure.
  • the rice bran wax oxidate (O) according to the invention is typically characterized by particularly good thermal stability, measured in accordance with DIN 51006 (2005) with a loss of mass up to a temperature of 300 ° C. (heating rate: 5 ° C./min) of less than 25%, preferably less than 20%, particularly preferably less than 17%.
  • the invention also relates to a saponified rice bran wax oxidate (V) produced by saponifying the rice bran wax oxidate (O) described above with a basic metal salt selected from the group consisting of metal hydroxides (e.g. NaOH, KOH, Ca (OH) 2 and Zn (OH) 2 , etc.), metal oxides (e.g. CaO, etc.), metal carbonates (e.g. Na2C03, CaC03, etc.) or with aqueous alkalis (such as NaOH, KOH, etc.).
  • a basic metal salt selected from the group consisting of metal hydroxides (e.g. NaOH, KOH, Ca (OH) 2 and Zn (OH) 2 , etc.), metal oxides (e.g. CaO, etc.), metal carbonates (e.g. Na2C03, CaC03, etc.) or with aqueous alkalis (such as NaOH, KOH, etc.).
  • the saponified products are preferably characterized by particularly good thermal stability, measured in accordance with DIN 51006 with a loss of mass up to a temperature of 300 ° C (heating rate: 5 ° C / min) of less than 10%, preferably less than 5%. out.
  • the invention also relates to the use of the rice bran wax oxidates (O) according to the invention or the saponified rice bran wax oxidates (V) according to the invention for agricultural or forestry purposes, as an additive in plastics processing, in care products, in printing inks and / or in paints.
  • the chain length distributions of the constituents of the rice bran wax oxidates were determined by means of gas chromatography. Served as comparison substances
  • Wax acids and wax alcohols with carbon chain lengths between C6 and C36 Wax esters with C44 to C58 were represented by combining the model substances.
  • a defined amount of the individual components was added to a wax sample and a significant increase in the area of the corresponding peak was observed. The measurement conditions are shown in Table 2.
  • Table 2 Rice bran wax (RBW 1) in its raw state was used as the raw material. The properties of the raw rice bran wax are shown in Table 3.
  • the organic phase was freed from chromium residues by washing with an aqueous solution of oxalic acid and sulfuric acid and then by washing with water, drained into warm centrifuge tubes and centrifuged.

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  • Oil, Petroleum & Natural Gas (AREA)
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Abstract

L'invention concerne des oxydats de cire de son de riz présentant un indice d'acide moyen, leur procédé de production et leur utilisation à des fins agricoles ou forestières, utilisés comme additif dans le traitement des matières plastiques, dans des produits de soins, dans des encres d'impression et/ou dans des peintures, et des oxydats de cire de son de riz saponifiés produits par saponification des oxydats de cire de son de riz selon les revendications.
PCT/EP2020/077785 2019-10-15 2020-10-05 Cire de son de riz brillant oxydée avec une teneur élevée en esterane WO2021073910A1 (fr)

Priority Applications (6)

Application Number Priority Date Filing Date Title
EP20781549.9A EP4045599A1 (fr) 2019-10-15 2020-10-05 Cire de son de riz brillant oxydée avec une teneur élevée en esterane
BR112022003064A BR112022003064A2 (pt) 2019-10-15 2020-10-05 Oxidados de cera de farelo de arroz claros com uma alta proporção de éster
CN202080072171.9A CN114555715B (zh) 2019-10-15 2020-10-05 具有高酯份额的浅色米糠蜡氧化物
JP2022521965A JP7470188B2 (ja) 2019-10-15 2020-10-05 高エステル含有率を有する明色米糠ワックス酸化物
US17/768,238 US20240117187A1 (en) 2019-10-15 2020-10-05 Bright rice bran wax oxidated with high esterane content
KR1020227016328A KR20220084345A (ko) 2019-10-15 2020-10-05 높은 에스테란 함량을 갖는 산화된 담색 쌀겨 왁스

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TW202116718A (zh) 2021-05-01
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